Brynes et al., 1978 - Google Patents
Potential antitumor agents via inhibitors of L‐asparagine synthetase: Substituted sulfonamides and sulfonyl hydrazides related to glutamineBrynes et al., 1978
- Document ID
- 14282600952527838332
- Author
- Brynes S
- Fiorina V
- Cooney D
- Milman H
- Publication year
- Publication venue
- Journal of Pharmaceutical Sciences
External Links
Snippet
A series of 4‐(substituted aminosulfonyl)‐and 4‐(substituted hydrazinosulfonyl)‐2‐ aminobutanoic acids, compounds structurally related to glutamine, was synthesized as potential inhibitors of L‐asparagine synthetase and subjected to screening as antitumor …
- 229960001230 Asparagine 0 title abstract description 15
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H19/00—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof
- C07H19/02—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing nitrogen
- C07H19/04—Heterocyclic radicals containing only nitrogen atoms as ring hetero atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US9487520B2 (en) | Coelenterazine derivatives and methods of using same | |
EP0243429B1 (en) | D-luciferin derivatives and their use | |
Högenauer | The mode of action of pleuromutilin derivatives: Location and properties of the pleuromutilin binding site on Escherichia coli ribosomes | |
US5686423A (en) | Di-and tri-peptide mimetic compounds for Parkinson's disease | |
US5880097A (en) | Tethered prodrugs | |
Brynes et al. | Potential antitumor agents via inhibitors of L‐asparagine synthetase: Substituted sulfonamides and sulfonyl hydrazides related to glutamine | |
Adams et al. | cis-4-Carboxy-6-(mercaptomethyl)-3, 4, 5, 6-tetrahydropyrimidin-2 (1H)-one, a potent inhibitor of mammalian dihydroorotase | |
Ishikawa et al. | Metabolism of benthiocarb (4-chlorobenzyl N, N-diethylthiolcarbamate) in mice | |
KR890001488B1 (en) | Method for preparing mitomycin C derivative | |
Vince et al. | Glutaryl-S-(p-bromobenzyl)-L-cysteinylglycine. Metabolically stable inhibitor of glyoxalase I | |
Liskamp et al. | Structure-activity relationships of sparsomycin and its analogs: octylsparsomycin: The first analog more active than sparsomycin | |
Matulic-Adamic et al. | Nucleosides. 150. Synthesis and some biological properties of 5-monofluoromethyl, 5-difluoromethyl, and 5-trifluoromethyl derivatives of 2'-deoxyuridine and 2'-deoxy-2'-fluoro-. beta.-D-arabinofuranosyluracil | |
CN1097761A (en) | Polycyclic compound and its preparation method | |
GB1582420A (en) | Phenylamino phenylacetic acid amide compounds and processes for their preparation | |
Mokotoff et al. | Potential inhibitors of L-asparagine biosynthesis. 5. Electrophilic amide analogs of (S)-2, 3-diaminopropionic acid | |
Schneller et al. | Biological activity and a modified synthesis of 8-amino-3-. beta.-D-ribofuranosyl-1, 2, 4-triazolo [4, 3-. alpha.] pyrazine, an isomer of formycin | |
US7342010B2 (en) | 2-thiaquinolizidines and process for the preparation thereof | |
US4581360A (en) | Sparsomycin (Sc -Rs) derivative; pharmaceutical composition having anti-tumor activity | |
JPH07316191A (en) | Acyloxyhexanoic acid derivative | |
Steinfeld et al. | Anticandidal activity of 5-fluorocytosine-peptide conjugates | |
HU198215B (en) | Process for production of compositions similar in construction with antibiotics tan-749 | |
Goldberg et al. | A dipeptide derived from kainic and L-glutamic acids: a selective antagonist of amino acid induced neuroexcitation with anticonvulsant properties | |
Nishihira et al. | Identification of the Electrophilic Substrate‐Binding Site of Glutathione S‐Transferase P by Photoaffinity Labeling | |
Liu et al. | Carbocyclic substrates for de novo purine biosynthesis. | |
US3573276A (en) | Alkylsulphonyl-cobalamines |